Suppr超能文献

经心肌内持续递送新型生长因子组合的动脉生成治疗可预防慢性心力衰竭。

Arteriogenic therapy by intramyocardial sustained delivery of a novel growth factor combination prevents chronic heart failure.

机构信息

Inserm U644, Institute for Biomedical Research, Rouen University, 22 Blvd Gambetta, 76183 Rouen, France.

出版信息

Circulation. 2011 Aug 30;124(9):1059-69. doi: 10.1161/CIRCULATIONAHA.110.010264. Epub 2011 Aug 8.

Abstract

BACKGROUND

Therapeutic angiogenesis is a promising approach for the treatment of cardiovascular diseases, including myocardial infarction and chronic heart failure. We aimed to improve proangiogenic therapies by identifying novel arteriogenic growth factor combinations, developing injectable delivery systems for spatiotemporally controlled growth factor release, and evaluating functional consequences of targeted intramyocardial growth factor delivery in chronic heart failure.

METHODS AND RESULTS

First, we observed that fibroblast growth factor and hepatocyte growth factor synergistically stimulate vascular cell migration and proliferation in vitro. Using 2 in vivo angiogenesis assays (n=5 mice per group), we found that the growth factor combination results in a more potent and durable angiogenic response than either growth factor used alone. Furthermore, we determined that the molecular mechanisms involve potentiation of Akt and mitogen-activated protein kinase signal transduction pathways, as well as upregulation of angiogenic growth factor receptors. Next, we developed crosslinked albumin-alginate microcapsules that sequentially release fibroblast growth factor-2 and hepatocyte growth factor. Finally, in a rat model of chronic heart failure induced by coronary ligation (n=14 to 15 rats per group), we found that intramyocardial slow release of fibroblast growth factor-2 with hepatocyte growth factor potently stimulates angiogenesis and arteriogenesis and prevents cardiac hypertrophy and fibrosis, as determined by immunohistochemistry, leading to improved cardiac perfusion after 3 months, as shown by magnetic resonance imaging. These multiple beneficial effects resulted in reduced adverse cardiac remodeling and improved left ventricular function, as revealed by echocardiography.

CONCLUSION

Our data showing the selective advantage of using fibroblast growth factor-2 together with hepatocyte growth factor suggest that this growth factor combination may constitute an efficient novel treatment for chronic heart failure.

摘要

背景

治疗性血管生成是治疗心血管疾病(包括心肌梗死和慢性心力衰竭)的一种很有前途的方法。我们旨在通过确定新的促血管生成生长因子组合、开发用于时空控制生长因子释放的可注射递送系统,以及评估靶向心肌内生长因子递送在慢性心力衰竭中的功能后果,来改善促血管生成疗法。

方法和结果

首先,我们观察到成纤维细胞生长因子和肝细胞生长因子协同刺激血管细胞的迁移和增殖。使用 2 种体内血管生成测定(每组 5 只小鼠),我们发现与单独使用任何一种生长因子相比,生长因子组合会产生更强大和更持久的血管生成反应。此外,我们确定其分子机制涉及 Akt 和丝裂原激活蛋白激酶信号转导途径的增强,以及促血管生成生长因子受体的上调。接下来,我们开发了交联的白蛋白-海藻酸盐微胶囊,可顺序释放成纤维细胞生长因子-2 和肝细胞生长因子。最后,在冠状动脉结扎诱导的大鼠慢性心力衰竭模型中(每组 14 至 15 只大鼠),我们发现成纤维细胞生长因子-2 与肝细胞生长因子的心肌内缓慢释放可强力刺激血管生成和生成动脉,并防止心脏肥大和纤维化,通过免疫组织化学检测,磁共振成像显示 3 个月后心脏灌注得到改善。这些多种有益作用导致心脏不良重塑减少,左心室功能改善,超声心动图显示。

结论

我们的数据显示,使用成纤维细胞生长因子-2 与肝细胞生长因子联合使用的选择性优势表明,这种生长因子组合可能构成慢性心力衰竭的有效新治疗方法。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验